Intracranial embolism

disease
On this page

Summary

Intracranial embolism (MONDO:0006809) is a disease and 8 clinical trials. Top therapeutic interventions include egaptivon pegol. A subtype of ischemic stroke — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 8

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameintracranial embolism
Mondo IDMONDO:0006809
EFOEFO:1000991
MeSHD020766
DOIDDOID:4372
ICD-11816982857
SNOMED CT75543006
UMLSC0752140
MedGen155710
Is cancer (heuristic)no

Disease family

This is a subtype of ischemic stroke. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › nervous system disordercentral nervous system disorderbrain disordercerebrovascular disorderstroke disorderischemic strokeintracranial embolism

Related subtypes (4): cerebral infarction, transient ischemic attack, brain stem infarction, pediatric arterial ischemic stroke

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 8.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified4
PHASE32
PHASE41
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00862160PHASE4UNKNOWNIncidence of Acute Cerebrovascular Events Using Either Minimized or Standard Cardiopulmonary Bypass Circuit
NCT00336596PHASE3UNKNOWNUltrasound Enhanced Thrombolytic Therapy of Middle Cerebral Artery Occlusion
NCT03001960PHASE3UNKNOWNDual AntiPlatelet Therapies for Prevention of Periinterventional Embolic Events in TAVI
NCT00742612PHASE2TERMINATEDEffect of ARC1779 on Cerebral Microembolism in Patients Undergoing Carotid Endarterectomy
NCT01752946Not specifiedUNKNOWNA Registry Study of Shuxuening Injection Used in Hospitals in China
NCT02321917Not specifiedCOMPLETEDRheoparin-coated Tubing System for Minimized Extracorporeal Circulation (MECC)
NCT02758964Not specifiedCOMPLETEDEvaluation of Cerebral Thrombembolism After TAVR
NCT02955004Not specifiedCOMPLETEDElectrical Cardioversion of Recent Onset Atrial Fibrillation - Silent Thromboembolic Events, Reverse Atrial Remodeling

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
EGAPTIVON PEGOL21

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.